Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

The Inscribed Polygon Method for Predicting Aromaticity

To fill the MOs, the six electrons are added, two to an orbital, beginning with the lowest energy orbital. As a result, the six electrons completely fill the bonding MOs, leaving the antibonding MOs empty. This is what gives benzene and other aromatic compounds their special stability and this is why six % electrons satisfies Hiickel s 4n + 2 rule. [Pg.629]

An inscribed poiygon is aiso caiied a Frost circle. [Pg.629]

HOW TO Use the Inscribed Polygon Method to Determine the Relative Energies of MOs for Cyclic, Completely Conjugated Compounds [Pg.629]

Step [1] Draw the polygon in question inside a circle with its vertices touching the circle and one of the vertices pointing down. Mark the points at which the polygon intersects the circle. [Pg.629]

Step [2] Draw a line horizontally through the center of the circle and label MOs as bonding, nonbonding, or antibonding. [Pg.629]

Step [3] Add the electrons, beginning with the lowest energy MO. [Pg.628]

Using the inscribed polygon method for five- and seven-membered rings [Pg.629]


See other pages where The Inscribed Polygon Method for Predicting Aromaticity is mentioned: [Pg.606]    [Pg.628]    [Pg.629]    [Pg.607]    [Pg.629]    [Pg.631]    [Pg.606]    [Pg.628]    [Pg.629]    [Pg.607]    [Pg.629]    [Pg.631]   


SEARCH



Aromaticity method

For prediction

Polygon method

Polygonization

© 2024 chempedia.info